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Ulerythema ophryogenes in Cornelia de Lange syndrome.
Pediatr Dermatol. 2002 Jan-Feb; 19(1):42-5.PD

Abstract

A 17-year-old woman with Cornelia de Lange syndrome had asymptomatic skin lesions since the age of 4 years. These were multiple, follicular, horny papules, present on both cheeks, and surrounded by erythematous skin. Similar lesions were present on the external aspect of the arms, but amidst skin of normal coloration. Keratosis pilaris atrophicans faciei (ulerythema ophryogenes) has been described as a cutaneous marker for several congenital syndromes. To our knowledge, its possible association with Cornelia de Lange syndrome has never been reported.

Authors+Show Affiliations

Department of Dermatology, Complejo Hospitalario Universitario, Faculty of Medicine, Santiago de Compostela, Spain. mejaime@usc.esNo affiliation info availableNo affiliation info available

Pub Type(s)

Case Reports
Journal Article

Language

eng

PubMed ID

11860570

Citation

Flórez, Angeles, et al. "Ulerythema Ophryogenes in Cornelia De Lange Syndrome." Pediatric Dermatology, vol. 19, no. 1, 2002, pp. 42-5.
Flórez A, Fernández-Redondo V, Toribio J. Ulerythema ophryogenes in Cornelia de Lange syndrome. Pediatr Dermatol. 2002;19(1):42-5.
Flórez, A., Fernández-Redondo, V., & Toribio, J. (2002). Ulerythema ophryogenes in Cornelia de Lange syndrome. Pediatric Dermatology, 19(1), 42-5.
Flórez A, Fernández-Redondo V, Toribio J. Ulerythema Ophryogenes in Cornelia De Lange Syndrome. Pediatr Dermatol. 2002 Jan-Feb;19(1):42-5. PubMed PMID: 11860570.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Ulerythema ophryogenes in Cornelia de Lange syndrome. AU - Flórez,Angeles, AU - Fernández-Redondo,Virginia, AU - Toribio,Jaime, PY - 2002/2/28/pubmed PY - 2002/5/1/medline PY - 2002/2/28/entrez SP - 42 EP - 5 JF - Pediatric dermatology JO - Pediatr Dermatol VL - 19 IS - 1 N2 - A 17-year-old woman with Cornelia de Lange syndrome had asymptomatic skin lesions since the age of 4 years. These were multiple, follicular, horny papules, present on both cheeks, and surrounded by erythematous skin. Similar lesions were present on the external aspect of the arms, but amidst skin of normal coloration. Keratosis pilaris atrophicans faciei (ulerythema ophryogenes) has been described as a cutaneous marker for several congenital syndromes. To our knowledge, its possible association with Cornelia de Lange syndrome has never been reported. SN - 0736-8046 UR - https://www.unboundmedicine.com/medline/citation/11860570/Ulerythema_ophryogenes_in_Cornelia_de_Lange_syndrome_ L2 - https://onlinelibrary.wiley.com/resolve/openurl?genre=article&sid=nlm:pubmed&issn=0736-8046&date=2002&volume=19&issue=1&spage=42 DB - PRIME DP - Unbound Medicine ER -